Disease: Encephalocele ×
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1553827236
rs1553827236
Entrez Id: 57545
Gene Symbol: CC2D2A
CC2D2A
CUI: C4551722
Disease:
Encephalocele 		A 0.700 CausalMutation CLINVAR